(S)-Boc-3-methoxy-β-Phe-OH

98%

Reagent Code: #60709
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CAS Number 499995-77-6

science Other reagents with same CAS 499995-77-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 295.33 g/mol
Formula C₁₅H₂₁NO₅
badge Registry Numbers
MDL Number MFCD03427899
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is widely used in peptide synthesis as a building block for creating complex peptide structures. It is particularly valuable in the preparation of peptides with specific stereochemistry, thanks to its chiral center. The Boc (tert-butoxycarbonyl) group serves as a protective group for the amine functionality, allowing selective reactions at other sites during peptide chain assembly. The methoxy group on the phenyl ring can influence the peptide's interaction with biological targets, making it useful in drug discovery and development. Additionally, it is employed in the synthesis of modified amino acids, which are critical in studying protein structure and function. Its applications extend to medicinal chemistry, where it is used to design and optimize bioactive peptides and peptidomimetics.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿4,671.00
100mg
10-20 days ฿1,080.00
250mg
10-20 days ฿1,710.00
(S)-Boc-3-methoxy-β-Phe-OH
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This chemical is widely used in peptide synthesis as a building block for creating complex peptide structures. It is particularly valuable in the preparation of peptides with specific stereochemistry, thanks to its chiral center. The Boc (tert-butoxycarbonyl) group serves as a protective group for the amine functionality, allowing selective reactions at other sites during peptide chain assembly. The methoxy group on the phenyl ring can influence the peptide's interaction with biological targets, making i

This chemical is widely used in peptide synthesis as a building block for creating complex peptide structures. It is particularly valuable in the preparation of peptides with specific stereochemistry, thanks to its chiral center. The Boc (tert-butoxycarbonyl) group serves as a protective group for the amine functionality, allowing selective reactions at other sites during peptide chain assembly. The methoxy group on the phenyl ring can influence the peptide's interaction with biological targets, making it useful in drug discovery and development. Additionally, it is employed in the synthesis of modified amino acids, which are critical in studying protein structure and function. Its applications extend to medicinal chemistry, where it is used to design and optimize bioactive peptides and peptidomimetics.

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